Canonical Allele Identifier: CA1519928187

Gene: F11

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186267387_186267388delinsCT , CM000666.2:g.186267387_186267388delinsCT	GRCh38
NC_000004.11:g.187188541_187188542delinsCT , CM000666.1:g.187188541_187188542delinsCT	GRCh37
NC_000004.10:g.187425535_187425536delinsCT	NCBI36
NG_008051.1:g.6424_6425delinsCT , LRG_583:g.6424_6425delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.55+196_55+197delinsCT MANE Select	ENSP00000384957.2:n.55+196_55+197delinsCT
ENST00000264692.8:c.55+196_55+197delinsCT	ENSP00000264692.5:n.55+196_55+197delinsCT
ENST00000403665.6:c.55+196_55+197delinsCT	ENSP00000384957.2:n.55+196_55+197delinsCT
ENST00000492972.6:c.55+196_55+197delinsCT	ENSP00000424479.1:n.55+196_55+197delinsCT
NM_000128.3:c.55+196_55+197delinsCT , LRG_583t1:c.55+196_55+197delinsCT	NP_000119.1:n.55+196_55+197delinsCT
XM_005262821.2:c.55+196_55+197delinsCT	XP_005262878.1:n.55+196_55+197delinsCT
XM_005262822.2:c.55+196_55+197delinsCT	XP_005262879.1:n.55+196_55+197delinsCT
XM_005262823.2:c.55+196_55+197delinsCT	XP_005262880.1:n.55+196_55+197delinsCT
XM_005262824.1:c.55+196_55+197delinsCT	XP_005262881.1:n.55+196_55+197delinsCT
XM_006714137.1:c.55+196_55+197delinsCT	XP_006714200.1:n.55+196_55+197delinsCT
XR_938706.1:n.407+196_407+197delinsCT
XR_938707.1:n.407+196_407+197delinsCT
NM_001354804.1:c.55+196_55+197delinsCT	NP_001341733.1:n.55+196_55+197delinsCT
XM_005262821.4:c.55+196_55+197delinsCT	XP_005262878.1:n.55+196_55+197delinsCT
XM_005262822.4:c.55+196_55+197delinsCT	XP_005262879.1:n.55+196_55+197delinsCT
XM_005262823.4:c.55+196_55+197delinsCT	XP_005262880.1:n.55+196_55+197delinsCT
XM_006714137.3:c.55+196_55+197delinsCT	XP_006714200.1:n.55+196_55+197delinsCT
XM_017007884.2:c.55+196_55+197delinsCT	XP_016863373.1:n.55+196_55+197delinsCT
XM_017007885.2:c.55+196_55+197delinsCT	XP_016863374.1:n.55+196_55+197delinsCT
XM_017007886.2:c.55+196_55+197delinsCT	XP_016863375.1:n.55+196_55+197delinsCT
XR_001741172.2:n.388+196_388+197delinsCT
NM_000128.4:c.55+196_55+197delinsCT MANE Select	NP_000119.1:n.55+196_55+197delinsCT
NM_001354804.2:c.55+196_55+197delinsCT	NP_001341733.1:n.55+196_55+197delinsCT